Kamikawa Y, Shimo Y
Br J Pharmacol. 1978 Dec;64(4):511-8. doi: 10.1111/j.1476-5381.1978.tb17312.x.
1 The effect of compound 48/80 was studied on the twitch-like contractions of the longitudinal muscle of guinea-pig ileum induced by electrical stimulation of intramural cholinergic nerves. 2 Compound 48/80 alone, at concentrations up to 30 microgram/ml, had no effect on the twitch contractions. The contraction to exogenously applied acetylcholine was slightly depressed by the compound. 3 At 100 microgram/ml, compound 48/80 caused a weak but long-lasting increase in tone and irregular contractile activity in the ileum, part of which was reduced but not completely abolished by pretreatment with chlorpheniramine (1 muM) or by repeated applications of compound 48/80. 4 The inhibitory effects of morphine and methionine-enkephalin on the twitches were antagonized by the presence of compound 48/80 (3 to 30 microgram/ml), possibly in a competitive manner. The antagonism was not affected by pretreatment with the antihistaminics, chlorpheniramine and/or metiamide. 5 The inhibitory effects of noradrenaline and adrenaline on the twitches were slightly but significantly increased by the presence of compound 48/80 (10 or 30 microgram/ml), whereas that of ATP was not modified. 6 Thesese results indicate that compound 48/80 acts as a selective and competitive antagonist at opiate receptors located in the intramural cholinergic nerves of guinea-pig ileum.
研究了化合物48/80对豚鼠回肠纵肌由壁内胆碱能神经电刺激诱导的类似抽搐收缩的影响。
单独使用浓度高达30微克/毫升的化合物48/80对抽搐收缩没有影响。该化合物对外源性应用的乙酰胆碱的收缩有轻微抑制作用。
在100微克/毫升时,化合物48/80使回肠张力出现微弱但持久的增加以及不规则的收缩活动,其中部分效应可被用氯苯那敏(1微摩尔)预处理或重复应用化合物48/80所减弱,但未完全消除。
化合物48/80(3至30微克/毫升)的存在拮抗了吗啡和甲硫氨酸脑啡肽对抽搐的抑制作用,可能是以竞争性方式。这种拮抗作用不受抗组胺药氯苯那敏和/或甲硫米特预处理的影响。
化合物48/80(10或30微克/毫升)的存在使去甲肾上腺素和肾上腺素对抽搐的抑制作用轻微但显著增强,而ATP的抑制作用未改变。
这些结果表明化合物48/80在豚鼠回肠壁内胆碱能神经中的阿片受体处起选择性和竞争性拮抗剂的作用。